Istraživači
Marjanović, Ana
Results 1-20 of 101
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2026 | Disease burden in Serbian patients with facioscapulohumeral muscular dystrophy![]() | Ralić, Branislav; Albano, Noemi; Virić, Vanja | Article | 22M22 |
| 2026 | Hidden diagnoses among patients with double seronegative myasthenia gravis![]() | Ivanović, Vukan | Article | 22M22 |
| 2025 | APOE, APP, and PSEN1 mutation screening in Alzheimer’s disease: a 15-year experience in Serbia![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2025 | Genetic and Clinical Insights into ALS/FTD: Profiling a Rare Cohort to Explore Spectrum Heterogeneity![]() | Marjanović, Ana | Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 2025 | APOE, ATXN1 and ATXN2 genetic analysis in ALS/FTD patients![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2025 | C9orf72–Associated ALS/FTD: From Genetic Diagnosis to Therapeutic Opportunities and Challenges![]() | Marjanović, Ana | Book parts | Mp. category will be shown later |
| 2025 | The role of genetic factors in the occurrence of levodopa-induced motor complications in Parkinson's disease![]() | Radojević, Branislava | Article | 22M22 |
| 2025 | The pleiotropy of C9orf72 repeat expansions in neurodegenerative diseases![]() | Marjanović, Ana | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2025 | Hereditary neuropathies in Serbian population![]() | Vukojević, Milica | Conference Paper | Mp. category will be shown later |
| 2025 | Secondary findings in 443 exome sequencing data![]() | Branković, Marija | Article | 23M23 |
| 2025 | Clinical exome sequencing identifies pathogenic SQSTM1 variant in a patient with chorea and gaze palsy![]() | Stojadinović, Lenka | Conference Paper | Mp. category will be shown later |
| 2025 | Frequency of TREM2 and APOE rare variants in patients with Alzheimer’s disease in Serbia![]() | Stojadinović, Lenka | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2025 | Chorea in Hereditary Leukodystrophies - Overview of Two Cases![]() | Milovanović, Andona | Naučni članak | 22M22 - Međunarodni časopis kategorije M22 |
| 2025 | Is GBA1 mutation status a game-changer for impulse control behaviour in Parkinson's disease?![]() | Kresojević, Nikola | Научни чланак | 22M22 - Међународни часопис категорије M22 |
| 2025 | Disease burden in Serbian patients with facioscapulohumeral muscular dystrophy![]() | Ralić, Branislav; Albano, N.; Virić, Vanja | Conference Paper | Mp. category will be shown later |
| 2024 | RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia![]() | Milovanović, Andona | Научни чланак | 21M21 |
| 2024 | Challenges in rare diseases: The example of mitochondrial diseases![]() | Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2024 | Distonija-ataksija sindrom ranog početka kao manifestacija POLR3a povezane leukodistrofije![]() | Šarčević, Maksim; Milovanović, Andona | Conference Paper | Mp. category will be shown later |
| 2024 | ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series![]() | Milovanović, Andona | Научни чланак | 21a+M21a+ - Водећи међународни часопис категорије M21a+ |
| 2024 | C9orf72 genetic screening in patients with ALS/FTD phenotype from Serbia![]() | Marjanović, Ana | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
